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. Author manuscript; available in PMC: 2015 Jan 14.
Published in final edited form as: Cell Signal. 2013 Jul 6;25(11):2163–2175. doi: 10.1016/j.cellsig.2013.07.002

Figure 2. Aldosterone induces TRPM7-dependent Mg2+ influx in HEK-293 cells.

Figure 2

HEK-293 cells expressing WT hTRPM7 channels or the mutants ΔKinase (deleted kinase) and K1648R (inactive kinase) were loaded with Mag-FURA-2 and were stimulated with 100 nM aldosterone in the absence or presence of the MR antagonist eplerenone (10 μM). Changes in Mag-FURA-2 fluorescence were recorded (excitation ratio: 340/380 nm). (A) Bar graph, Mag-FURA-2 fluorescence ratio peak obtained after aldosterone stimulation. (B) Bar graph, Mag-FURA-2 fluorescence ratio peak obtained after aldosterone stimulation in the absence and in presence of eplerenone. Top panels, representative images of aldosterone effect on Mag-FURA-2 fluorescence intensity. Results are expressed as mean ± SE of 6-8 independent experiments.*p<0.05, versus corresponding basal levels; **p <0.05, aldosterone in the absence versus presence of eplerenone.